Speaking of Pfizer executives on the run - has Pfizer reported to the FDA about the increased risk of heart damage after its mRNA shot?

From here:

Deadline Passes for Pfizer to Submit Results of Post-Vaccination Heart Inflammation Study to US Regulators (theepochtimes.com)

“According to the FDA, Pfizer had until June 30, 2022, to complete the study and then another six months to prepare and submit the final results.”

“.. regulators determined that without the studies, there would not be sufficient data to assess the “known serious risks of myocarditis and pericarditis,” or heart inflammation ..and a related condition.. Regulators were also concerned about the potential risk of subclinical myocarditis, or heart inflammation without typical symptoms.”

Pfizer may have actually submitted a report. Neither the FDA or Pfizer has commented.

“..according to Jessica Adams, a former regulatory officer at the FDA. “We shouldn’t have to ask or demand this information. We should expect that it’d be promptly shared by default,” Adams wrote on Twitter.”

Dr. Janet Woodcock, the agency’s principal deputy director, told Adams in an email that the FDA is “not allowed to comment on potential actions on regulated products.”

“U.S. authorities, and some officials elsewhere, have since acknowledged that the vaccines cause heart inflammation. “The current evidence supports a causal association between mRNA COVID-19 vaccination and myocarditis and pericarditis,” Dr. Tom Shimabukuro, a top CDC official, said during a meeting in 2022.”

Onwards!

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